Search Results: 29,423 vacancies
...the study specific eTMF plans for assigned clinical studies.
Perform quality control of... ...established acceptable criteria
Ensure clinical trial documentation is consistent with eTMF... ...~3+ years of relevant clinical research and TMF experience at a biotechnology, pharmaceutical...
...We are seeking a highly motivated and detail-oriented Clinical Research Associate Intern to join our team. This internship provides a hands-on learning experience within the dynamic field of clinical trials. You will gain exposure to the essential processes involved in conducting...
...Clinical Research Associate
Responsibilities:
Pre-Trial:
Identify and qualify potential clinical trial sites and investigators.
Set up and equip trial sites with necessary materials and equipment.
Train site staff on study procedures and data collection methods...
...Summary:
We are seeking a highly motivated and experienced Clinical Research Associate (CRA) with a minimum of 2-3 years of relevant experience.... ...successful planning, execution, and monitoring of clinical trials. The ideal candidate will have a strong understanding of clinical...
...We have many new ground-breaking global clinical trial projects in various phases and therapeutic... ...are we?
~ A leading global clinical research organization founded in Asia-Pacific driven... ...role:
The Senior Clinical Research Associate (SCRA) is a member of the Clinical Operations...
...Responsibilities
Support CRAs with the setup monitoring and closeout of clinical trials in accordance with Good Clinical Practice (GCP) ICH guidelines... ...Biology Nursing Public Health
Strong interest in clinical research and drug development.
Excellent organizational and time...
...documents are available for filing in the Trial Master File (TMF) and verify that... ...to monitoring and study plan
Support clinical quality in managing CAPAs and other study... ...in clinical trials industry as Clinical Research Associate
Good working knowledge of GCP and local...
...Post : Clinical Research Associate/Clinical Trial
Location : Ahmedabad-(Science City Road, Sola)
Exp : 3Yrs to 8Yrs
Roles & Responsibilities:
- Perform on-site in-process and retrospective monitoring visit of clinical phase of the clinical trials, PK and BA/BE studies...
...ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving... ...mission to shape the future of clinical development.
Clinical Trial Assistant
Location : Mumbai, Office based...
...Clinical Data Management (CDM)
Clinical Data Managers (CDMs) are responsible for ensuring the accuracy, integrity, and completeness of data collected in clinical trials. They work closely with clinical investigators, statisticians, and other members of the clinical trial...
...Job Description
ICON plc is a world-leading healthcare intelligence and clinical research organization. From molecule to medicine, we advance clinical research providing outsourced services to pharmaceutical, biotechnology, medical device and government and public health...
..., Collaboration, Partnership and Integrity. We want to be the Clinical Research Organisation that delivers excellence to our clients and to patients... ...activity or lack thereof which may jeopardise the clinical trial delivery or patient safety .
• *Ensure all necessary...
...Overview: As a Clinical Research Associate (CRA), you will play a pivotal role in the development and execution of clinical trials Working closely with research teams, regulatory bodies, and clinical sites, you will ensure compliance with protocols, regulatory requirements...
...of the LCTL/CTL, as assigned. Support the clinical protocol development process in... ...and related documents; drive and/or supprt trial-related documents and processes.
development... ...Management Department as well as with the Assay Research Lab. This also includes the set-up,...
...TMF Specialist Responsibilities:
Receive and process clinical trial documents, ensuring proper filing and indexing.
Perform quality... ...Collaborate with cross-functional teams, including clinical research associates, data managers, and regulatory affairs specialists.
Stay...
...About the job
Summary
Monitors patient data study-related information related to clinical study sites and clinical trial participation.. Ensures the investigator adheres to research protocols, regulatory requirements and good clinical practices and provides input into...
...Job Description
We're looking for a proactive and highly communicative clinical research professional, pivotal in critically analyzing and summarizing clinical literature to provide valuable insights. Collaborating with cross-functional teams, you will contribute to the...
...to ensure that people living with a chronic disease can live a full life. We are looking for a dedicated EU Submission Lead for Clinical Trials to join our Global Regulatory Affairs team.
If you are passionate about driving change and navigating complex agendas, apply today...
About the job
Job Description Senior Business Analyst
Required Skills:
5+ years of experience with minimal 4-year experience in Client Management and Business/System Analysis Role.
At least 3 year of experience in HealthCare or Pharmaceutical (CRO) industry.
...
...We are looking for an organized, flexible Clinical Research Associate to oversee clinical trials. The Clinical Research Associate will develop and outline trial protocols, establish trial sites, train site staff, and manage Investigational Product (IP) and trial materials....
